Noonan syndrome with multiple lentigines

A RASopathy that is characterized by autosomal dominant inheritance of brown skin spots called lentigines that are similar to freckles, heart defects, widely spaced eyes a sunken chest or protruding chest and short stature.

Also known as: Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome; Generalized lentiginosis; Gorlin syndrome II; LEOPARD syndrome; Lentiginosis profusa syndrome